CA2295017A1 - Process for preparing enantiomerically enriched n-derivatised lactams - Google Patents

Process for preparing enantiomerically enriched n-derivatised lactams Download PDF

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Publication number
CA2295017A1
CA2295017A1 CA002295017A CA2295017A CA2295017A1 CA 2295017 A1 CA2295017 A1 CA 2295017A1 CA 002295017 A CA002295017 A CA 002295017A CA 2295017 A CA2295017 A CA 2295017A CA 2295017 A1 CA2295017 A1 CA 2295017A1
Authority
CA
Canada
Prior art keywords
azabicyclo
hept
protected
formula
reaction
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
CA002295017A
Other languages
English (en)
French (fr)
Inventor
Michael John Dawson
Mahmoud Mahmoudian
Christopher John Wallis
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Glaxo Group Ltd
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Publication of CA2295017A1 publication Critical patent/CA2295017A1/en
Abandoned legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P41/00Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P13/00Preparation of nitrogen-containing organic compounds
    • C12P13/02Amides, e.g. chloramphenicol or polyamides; Imides or polyimides; Urethanes, i.e. compounds comprising N-C=O structural element or polyurethanes
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/52Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring condensed with a ring other than six-membered
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P41/00Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture
    • C12P41/006Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by reactions involving C-N bonds, e.g. nitriles, amides, hydantoins, carbamates, lactames, transamination reactions, or keto group formation from racemic mixtures
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/55Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Wood Science & Technology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Zoology (AREA)
  • Health & Medical Sciences (AREA)
  • General Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Biotechnology (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Microbiology (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Analytical Chemistry (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Hydrogenated Pyridines (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
CA002295017A 1997-08-22 1998-08-20 Process for preparing enantiomerically enriched n-derivatised lactams Abandoned CA2295017A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GBGB9717928.7A GB9717928D0 (en) 1997-08-22 1997-08-22 Process for the enatioselective hydrolysis of n-derivatised lactams
GB9717928.7 1997-08-22
PCT/EP1998/005291 WO1999010519A1 (en) 1997-08-22 1998-08-20 Process for preparing enantiomerically enriched n-derivatised lactams

Publications (1)

Publication Number Publication Date
CA2295017A1 true CA2295017A1 (en) 1999-03-04

Family

ID=10817952

Family Applications (1)

Application Number Title Priority Date Filing Date
CA002295017A Abandoned CA2295017A1 (en) 1997-08-22 1998-08-20 Process for preparing enantiomerically enriched n-derivatised lactams

Country Status (35)

Country Link
US (1) US6340587B1 (no)
EP (1) EP1003903B1 (no)
JP (1) JP3565868B2 (no)
KR (1) KR100479894B1 (no)
CN (1) CN1133749C (no)
AP (1) AP1104A (no)
AR (1) AR016395A1 (no)
AT (1) ATE233323T1 (no)
AU (1) AU738897B2 (no)
BR (1) BR9810472B1 (no)
CA (1) CA2295017A1 (no)
CZ (1) CZ294302B6 (no)
DE (1) DE69811677T2 (no)
DK (1) DK1003903T3 (no)
EA (1) EA001964B1 (no)
EE (1) EE03934B1 (no)
ES (1) ES2193568T3 (no)
GB (1) GB9717928D0 (no)
HK (1) HK1025796A1 (no)
HR (1) HRP990408B1 (no)
HU (1) HU222657B1 (no)
ID (1) ID25830A (no)
IL (1) IL133541A (no)
IN (1) IN183908B (no)
IS (1) IS2201B (no)
NO (1) NO320081B1 (no)
NZ (1) NZ501880A (no)
PL (1) PL191108B1 (no)
PT (1) PT1003903E (no)
RS (1) RS49542B (no)
SI (1) SI1003903T1 (no)
SK (1) SK282782B6 (no)
TR (1) TR199903210T2 (no)
TW (1) TW589301B (no)
WO (1) WO1999010519A1 (no)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1095160B1 (de) * 1998-07-09 2004-01-28 Lonza AG Verfahren zur herstellung von (1r,4s)-2-azabicyclo 2.2.1 hept-5-en-3-on-derivaten
DE19962543A1 (de) * 1999-12-23 2001-07-05 Degussa Chromatographische Enantiomerentrennung von bicyclischen Lactamen
US6780635B2 (en) * 2001-12-27 2004-08-24 Council Of Scientific And Industrial Research Process for the preparation of optically active azabicyclo heptanone derivatives
EP1348765B1 (en) * 2002-03-28 2006-05-24 Council of Scientific and Industrial Research Process for the preparation of optically active azabicyclo heptanone derivatives
HU227663B1 (en) * 2007-07-09 2011-10-28 Univ Szegedi Resolution process
TR201807704T4 (tr) 2010-01-27 2018-06-21 Viiv Healthcare Co Anti-viral tedavi.
CN103695495B (zh) * 2014-01-14 2014-08-27 营口三征新科技化工有限公司 一种制备(1R,4s)-(-)-2-氮杂双环[2,2,1]庚-5-烯-3-酮的方法

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DK0424064T3 (da) * 1989-10-16 1995-06-26 Chiroscience Ltd Chirale azabicycloheptanoner og fremgangsmåde til fremstilling deraf
GB9108384D0 (en) 1991-04-19 1991-06-05 Enzymatix Ltd Bicycloheptanes
SK284810B6 (sk) * 1997-05-13 2005-12-01 Lonza Ag Spôsob výroby (1S,4R)- alebo (1R,4S)-4-(2-amino-6-chlór-9-H- purín-9-yl)-2-cyklopentén-1-metanolu

Also Published As

Publication number Publication date
CN1133749C (zh) 2004-01-07
HRP990408A2 (en) 2000-04-30
NO996368L (no) 2000-02-21
BR9810472B1 (pt) 2011-01-11
JP3565868B2 (ja) 2004-09-15
DE69811677T2 (de) 2003-10-16
IN183908B (no) 2000-05-13
JP2001504354A (ja) 2001-04-03
HRP990408B1 (en) 2006-05-31
DE69811677D1 (de) 2003-04-03
PL191108B1 (pl) 2006-03-31
GB9717928D0 (en) 1997-10-29
HUP0002661A3 (en) 2001-12-28
EA199901059A1 (ru) 2000-08-28
AU9738698A (en) 1999-03-16
HUP0002661A2 (hu) 2000-12-28
CN1261405A (zh) 2000-07-26
IL133541A (en) 2003-10-31
NZ501880A (en) 2001-08-31
EP1003903A1 (en) 2000-05-31
AP1104A (en) 2002-09-04
PT1003903E (pt) 2003-06-30
EE200000075A (et) 2000-10-16
EE03934B1 (et) 2002-12-16
TW589301B (en) 2004-06-01
AU738897B2 (en) 2001-09-27
KR100479894B1 (ko) 2005-03-30
HU222657B1 (hu) 2003-09-29
EP1003903B1 (en) 2003-02-26
BR9810472A (pt) 2000-09-19
AR016395A1 (es) 2001-07-04
HK1025796A1 (en) 2000-11-24
KR20010014078A (ko) 2001-02-26
SI1003903T1 (en) 2003-08-31
EA001964B1 (ru) 2001-10-22
ES2193568T3 (es) 2003-11-01
YU69399A (sh) 2002-06-19
PL337647A1 (en) 2000-08-28
IS2201B (is) 2007-02-15
WO1999010519A1 (en) 1999-03-04
IS5297A (is) 1999-12-14
RS49542B (sr) 2007-02-05
ATE233323T1 (de) 2003-03-15
US6340587B1 (en) 2002-01-22
CZ471699A3 (cs) 2000-06-14
IL133541A0 (en) 2001-04-30
NO996368D0 (no) 1999-12-21
NO320081B1 (no) 2005-10-17
SK184499A3 (en) 2000-09-12
TR199903210T2 (xx) 2000-07-21
DK1003903T3 (da) 2003-06-10
AP9901721A0 (en) 1999-12-31
CZ294302B6 (cs) 2004-11-10
ID25830A (id) 2000-11-09
SK282782B6 (sk) 2002-12-03

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Legal Events

Date Code Title Description
EEER Examination request
FZDE Discontinued